Big enough to include the specialists you need, small enough to really care
RSA is a first class regulatory science consultancy business, co-ordinating individual specialist skills, capitalising on their combined value to meet the individual needs of each client. With decades of industry experience, RSA are an enthusiastic and dedicated team of highly qualified toxicological, risk assessors, regulatory affairs specialists and Project Managers. Whether working independently or as part of your own project team, RSA’s world-class consultants are committed to providing you with the support that will address and resolve complex issues.
RSA was founded in 2007 by co-Directors Charlotte Croudace (Director, Regulatory Affairs) and Dr Mac Provan (Director, Toxicology). RSA aims to provide world-class toxicology, safety science and regulatory support, via expert associates, to a range of Industry sectors.
RSA consultants have a broad experience of addressing regulatory and specialist toxicology issues in regulatory environments world-wide, with particular focus on registration within Europe.
RSA are an enthusiastic and dedicated team of highly qualified and reputable toxicologists, regulatory affairs specialists and PMs
RSA can cover a number of sectors and specialisms with our dynamic, experienced team.
RSA has extensive experience in gaining and maintaining product registrations in the EU and US. Our respected experts bring together high-quality scientific expertise and in-depth knowledge of regulatory processes to ensure the optimum outcomes for our clients. From data-gap analysis and Study Monitoring of toxicology packages, through project management, preparation of regulatory documents, advocacy and representation through regulatory processes, RSA provides a comprehensive package of techno-regulatory services.
RSA has a proven track record of providing expert advice, the requisite documentation and direct technical support opposite the requirements of REACH. RSA is a member/technical lead provider on a number of industry consortia, and was instrumental in helping many companies meet the requirements for the 2010 deadlines, and beyond. As the 2018 deadlines for lower tonnage chemicals approaches, RSA can help and advise on classification and labelling under CLP.
RSA has a number of highly experienced consultants with decades of experience of taking drugs from discovery through clinical development and on to the market. Our expertise includes Toxicology, Pathology, Drug Metabolism and Environmental specialist areas. From Study Monitoring individual studies or designing non-clinical safety packages, to authoring and defending regulatory submissions worldwide, RSA can help clients to accelerate development, reduce costs and reach the market sooner.
Expertise Our consultants offer expertise in the following areas, see our expertise page to see who can best assist you
Metabolism and Kinetics
Services Our consultants offer the following services
Pathology slide reading and peer review
Mode of Action/weight of evidence assessments
Data gap analysis
Regulatory document preparation
RSA’s world-class consultants are committed to providing you with the support that will address and resolve complex issues.